Division of Psychiatry and Applied Psychology, School of Medicine, University of Nottingham, Nottingham, UK.
School of Health, Wellbeing and Social Care, The Open University, Milton Keynes, UK.
Int Psychogeriatr. 2021 Nov;33(11):1161-1192. doi: 10.1017/S1041610221000119. Epub 2021 Mar 17.
Disclosing a diagnosis of dementia is a key process involving people with dementia, carers, and healthcare professionals (HCPs) that can facilitate access to treatment and support. Receiving a diagnosis of dementia may represent a change in identity and loss of a planned-for future, resulting in an emotional impact for both people with dementia and carers. Delivering the diagnosis of dementia can be difficult and draining for HCPs.
We conducted a systematic review that included studies which explored the experience of giving or receiving a diagnosis of dementia from the perspectives of people with dementia, carers, or HCPs. All study designs were eligible except for previous literature reviews. Findings were analyzed thematically and grouped into categories and then synthesized into a narrative review. The quality of all included studies was assessed.
Fifty-two studies were included in this review. Findings indicated that receiving a diagnosis is generally a negative process for people with dementia, carers, and HCPs and leaves carers in particular feeling uncertain over the prognosis and future of the person they care for. Disclosing a diagnosis of dementia is a difficult and complex process, for which formal training and guidance is lacking. Carers in particular would welcome more opportunity for realistic and hopeful discussions of the implications of receiving a diagnosis of dementia.
Changes in some aspects of disclosure, such as providing a truthful diagnosis to the person with dementia, have occurred over the last decade. A process approach involving pre-diagnostic counseling and follow-up appointments could enable discussions regarding prognosis and the future, create opportunities to clarify the diagnosis, and reduce emotional burden on HCPs. There is a need for more objective evidence that considers the perspectives of all individuals involved.
向痴呆症患者、照顾者和医疗保健专业人员(HCP)披露痴呆症诊断是一个关键过程,这有助于他们获得治疗和支持。诊断痴呆症可能代表着身份的改变和对未来计划的丧失,从而对痴呆症患者和照顾者产生情感影响。向 HCP 提供痴呆症诊断可能很困难,也会让他们感到精疲力竭。
我们进行了一项系统评价,其中包括探索痴呆症患者、照顾者或 HCP 从自身角度获得或提供痴呆症诊断的经验的研究。所有研究设计均符合条件,除了以前的文献综述。研究结果进行了主题分析,并分为类别,然后综合成叙述性综述。所有纳入研究的质量都进行了评估。
本综述纳入了 52 项研究。研究结果表明,对痴呆症患者、照顾者和 HCP 来说,获得诊断通常是一个负面的过程,这让照顾者特别对他们所照顾的人的预后和未来感到不确定。披露痴呆症诊断是一个困难且复杂的过程,目前缺乏正式的培训和指导。特别是照顾者,他们更希望有机会对接受痴呆症诊断的影响进行现实和有希望的讨论。
在过去十年中,在一些披露方面发生了变化,例如向痴呆症患者提供真实的诊断。通过预诊断咨询和后续预约的过程方法,可以使人们有机会讨论预后和未来,澄清诊断,并减轻 HCP 的情绪负担。需要更多考虑所有相关个体观点的客观证据。